Genomics and Models of Nerve Sheath Tumors (Record no. 3008914)

MARC details
000 -LEADER
fixed length control field 04138naaaa2200889uu 4500
001 - CONTROL NUMBER
control field https://directory.doabooks.org/handle/20.500.12854/69300
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20220714185655.0
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number books978-3-03943-490-9
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 9783039434893
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 9783039434909
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.3390/books978-3-03943-490-9
Terms of availability doi
041 0# - LANGUAGE CODE
Language code of text/sound track or separate title English
042 ## - AUTHENTICATION CODE
Authentication code dc
072 #7 - SUBJECT CATEGORY CODE
Subject category code M
Source bicssc
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name Hirbe, Angela C.
Relator code edt
9 (RLIN) 1608912
245 10 - TITLE STATEMENT
Title Genomics and Models of Nerve Sheath Tumors
260 ## - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT)
Place of publication, distribution, etc Basel, Switzerland
Name of publisher, distributor, etc MDPI - Multidisciplinary Digital Publishing Institute
Date of publication, distribution, etc 2020
300 ## - PHYSICAL DESCRIPTION
Extent 1 electronic resource (172 p.)
506 0# - RESTRICTIONS ON ACCESS NOTE
Terms governing access Open Access
Source of term star
Standardized terminology for access restriction Unrestricted online access
520 ## - SUMMARY, ETC.
Summary, etc Nerve sheath tumors can be a significant cause of morbidity for many patients. These include benign tumors such as schwannomas, diffuse and plexiform neurofibromas, and atypical neurofibromas, as well as the aggressive soft tissue sarcoma known as the malignant peripheral nerve sheath tumor (MPNST). Nerve sheath tumors occur sporadically and in the context of the clinical neuro-genetic tumor predisposition syndromes neurofibromatosis type 1 (NF1) and type 2 (NF2). Historically, the mainstay of treatment for nerve sheath tumors has been surgery. However, for both benign and malignant nerve sheath tumors, there is a high recurrence rate, highlighting the pressing need for novel therapies. As we have entered the genomic era, the hope is that an improved understanding of the genetics, and therefore the biology, of these tumors will ultimately lead to therapies that result in better outcomes. In this Special Issue, we include both review articles and original research related to the genomic understanding and modeling of schwannomas, plexiform and diffuse neurofibromas, atypical neurofibromas, and malignant peripheral nerve sheath tumors as well as genomic methods being developed and applied to advance our understanding of these tumors.
540 ## - TERMS GOVERNING USE AND REPRODUCTION NOTE
Terms governing use and reproduction Creative Commons
-- https://creativecommons.org/licenses/by/4.0/
-- cc
-- https://creativecommons.org/licenses/by/4.0/
546 ## - LANGUAGE NOTE
Language note English
650 #7 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name as entry element Medicine
Source of heading or term bicssc
653 ## - INDEX TERM--UNCONTROLLED
Uncontrolled term neurofibromatosis type 1
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Uncontrolled term nerve sheath tumor
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Uncontrolled term cancer
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Uncontrolled term latent variables
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Uncontrolled term machine learning
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Uncontrolled term supervised learning
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Uncontrolled term transfer learning
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Uncontrolled term random forest
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Uncontrolled term metaVIPER
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Uncontrolled term tumor deconvolution
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Uncontrolled term neurofibromatosis
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Uncontrolled term malignant peripheral nerve sheath tumor
653 ## - INDEX TERM--UNCONTROLLED
Uncontrolled term MPNST
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Uncontrolled term polycomb repressive complex
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Uncontrolled term PRC2
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Uncontrolled term NF1
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Uncontrolled term kinase
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Uncontrolled term kinome adaptation
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Uncontrolled term kinome reprogramming
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Uncontrolled term MET
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Uncontrolled term MEK
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Uncontrolled term doxorubicin
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Uncontrolled term capmatinib
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Uncontrolled term genomics
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Uncontrolled term tumor evolution
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Uncontrolled term pathology
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Uncontrolled term next generation sequencing
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Uncontrolled term clinical genetics
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Uncontrolled term malignant peripheral nerve sheath tumors
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Uncontrolled term plexiform neurofibromas
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Uncontrolled term Schwann cells
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Uncontrolled term neurofibromatosis type 1 syndrome
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Uncontrolled term neurofibromin 1
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Uncontrolled term genetically engineered mouse models
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Uncontrolled term heterogeneity
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Uncontrolled term CRISPR/Cas9
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Uncontrolled term mouse models
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Uncontrolled term sarcoma
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Uncontrolled term tumor microenvironment
653 ## - INDEX TERM--UNCONTROLLED
Uncontrolled term neurofibromatosis 1 (NF1)
653 ## - INDEX TERM--UNCONTROLLED
Uncontrolled term mebendazole (MBZ)
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Uncontrolled term COX-2 inhibitor
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Uncontrolled term malignancy
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Uncontrolled term chemoprevention
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Uncontrolled term nerve sheath tumors
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Pratilas, Christine A.
Relator code edt
9 (RLIN) 1608913
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Dodd, Rebecca D.
Relator code edt
9 (RLIN) 1608914
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Hirbe, Angela C.
Relator code oth
9 (RLIN) 1608912
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Pratilas, Christine A.
Relator code oth
9 (RLIN) 1608913
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Dodd, Rebecca D.
Relator code oth
9 (RLIN) 1608914
856 40 - ELECTRONIC LOCATION AND ACCESS
Host name www.oapen.org
Uniform Resource Identifier <a href="https://mdpi.com/books/pdfview/book/3090">https://mdpi.com/books/pdfview/book/3090</a>
-- 0
Public note DOAB: download the publication
856 40 - ELECTRONIC LOCATION AND ACCESS
Host name www.oapen.org
Uniform Resource Identifier <a href="https://directory.doabooks.org/handle/20.500.12854/69300">https://directory.doabooks.org/handle/20.500.12854/69300</a>
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Public note DOAB: description of the publication
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